Browse DCSTAMP

Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Basic function annotation.
> Subcellular Location, Domain and Function
> Gene Ontology
> KEGG and Reactome Pathway
> Subcellular Location, Domain and Function
 
Subcellular Location Cell membrane Multi-pass membrane protein Endoplasmic reticulum membrane; Multi-pass membrane protein. Endoplasmic reticulum-Golgi intermediate compartment membrane Multi-pass membrane protein Endosome Note=Localizes to the cell surface in osteoclasts and undifferentiated monocytes. Intracellular internalized DCSTAMP is detected in a fraction of RANKL-induced osteoclast precursor. Colocalizes with OS9 in the endoplasmic reticulum (ER) of immature dendritic cell (DC). Translocates from the endoplasmic reticulum to the intermediate/Golgi compartment upon maturation of DC in a OS9-dependent manner. Colocalizes with LAMP1 in endosomes (By similarity).
Domain PF07782 DC-STAMP-like protein
Function

Probable cell surface receptor that plays several roles in cellular fusion, cell differentiation, bone and immune homeostasis. Plays a role in TNFSF11-mediated osteoclastogenesis. Cooperates with OCSTAMP in modulating cell-cell fusion in both osteoclasts and foreign body giant cells (FBGCs). Participates in osteoclast bone resorption. Involved in inducing the expression of tartrate-resistant acid phosphatase in osteoclast precursors. Plays a role in haematopoietic stem cell differentiation of bone marrow cells toward the myeloid lineage. Inhibits the development of neutrophilic granulocytes. Plays also a role in the regulation of dendritic cell (DC) antigen presentation activity by controlling phagocytic activity. Involved in the maintenance of immune self-tolerance and avoidance of autoimmune reactions.

> Gene Ontology
 
Biological Process GO:0000768 syncytium formation by plasma membrane fusion
GO:0001558 regulation of cell growth
GO:0001773 myeloid dendritic cell activation
GO:0001894 tissue homeostasis
GO:0002274 myeloid leukocyte activation
GO:0002521 leukocyte differentiation
GO:0002573 myeloid leukocyte differentiation
GO:0002761 regulation of myeloid leukocyte differentiation
GO:0002763 positive regulation of myeloid leukocyte differentiation
GO:0006949 syncytium formation
GO:0016049 cell growth
GO:0030099 myeloid cell differentiation
GO:0030224 monocyte differentiation
GO:0030308 negative regulation of cell growth
GO:0030316 osteoclast differentiation
GO:0032844 regulation of homeostatic process
GO:0032846 positive regulation of homeostatic process
GO:0034103 regulation of tissue remodeling
GO:0034105 positive regulation of tissue remodeling
GO:0034238 macrophage fusion
GO:0034239 regulation of macrophage fusion
GO:0034241 positive regulation of macrophage fusion
GO:0034612 response to tumor necrosis factor
GO:0036005 response to macrophage colony-stimulating factor
GO:0036006 cellular response to macrophage colony-stimulating factor stimulus
GO:0043011 myeloid dendritic cell differentiation
GO:0045124 regulation of bone resorption
GO:0045453 bone resorption
GO:0045637 regulation of myeloid cell differentiation
GO:0045639 positive regulation of myeloid cell differentiation
GO:0045655 regulation of monocyte differentiation
GO:0045657 positive regulation of monocyte differentiation
GO:0045780 positive regulation of bone resorption
GO:0045926 negative regulation of growth
GO:0046849 bone remodeling
GO:0046850 regulation of bone remodeling
GO:0046852 positive regulation of bone remodeling
GO:0048771 tissue remodeling
GO:0048871 multicellular organismal homeostasis
GO:0060142 regulation of syncytium formation by plasma membrane fusion
GO:0060143 positive regulation of syncytium formation by plasma membrane fusion
GO:0060249 anatomical structure homeostasis
GO:0061025 membrane fusion
GO:0070670 response to interleukin-4
GO:0071353 cellular response to interleukin-4
GO:0071356 cellular response to tumor necrosis factor
GO:0072674 multinuclear osteoclast differentiation
GO:0072675 osteoclast fusion
GO:0097028 dendritic cell differentiation
GO:1902105 regulation of leukocyte differentiation
GO:1902107 positive regulation of leukocyte differentiation
GO:1903131 mononuclear cell differentiation
GO:1903706 regulation of hemopoiesis
GO:1903708 positive regulation of hemopoiesis
Molecular Function -
Cellular Component GO:0005793 endoplasmic reticulum-Golgi intermediate compartment
GO:0010008 endosome membrane
GO:0030176 integral component of endoplasmic reticulum membrane
GO:0031227 intrinsic component of endoplasmic reticulum membrane
GO:0033116 endoplasmic reticulum-Golgi intermediate compartment membrane
GO:0044440 endosomal part
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between DCSTAMP and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells.
> Text Mining
 

There is no record.

Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets.
> High-throughput Screening
  Statistical results of DCSTAMP in screening data sets for detecting immune reponses.
PMID Screening System Cancer Type Cell Line Data Set Statistical Results Relation to immunity
29301958CRISPR-Cas9 melanomaB16F10Pmel-1 T cell NA/NSNA/NS
29301958CRISPR-Cas9 melanomaB16F10OT-1 T cell NA/NSNA/NS
28783722CRISPR-Cas9 melanomaMel6242CT-CRISPR NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX+Anti-PD1 NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX NA/NSNA/NS
25691366RNAiBreast cancerMCF7Luc-CTL assay NA/NSNA/NS
24476824shRNAmelanomaB16Primary screen NA/NSNA/NS
24476824shRNAmelanomaB16Secondary screen NA/NSNA/NS
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets.
> Expression difference between responders and non-responders
> Mutation difference between responders and non-responders
> Expression difference between responders and non-responders
 
Points in the above scatter plot represent the expression difference of DCSTAMP in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-1.6190.0162
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-2.4680.0252
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-10.305
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 916-1.5020.0815
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-1.3040.312
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47-1.750.238
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.5710.471
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-1.8660.0942
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11121.0230.39
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 480.0030.996
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 280.8760.255
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 682300.0220.94
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of DCSTAMP in various data sets.
No PMID Cancer type Group Drug # Res # NRes % Mut/Res % Mut/NRes % Diff (R vs NR) Pval Anno
125765070Non-small cell lung cancer (NSCLC)allAnti-PD-1 (pembrolizumab) 14177.15.91.21
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 103100101
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 41407.1-7.11
426359337MelanomaallAnti-CTLA-4 (ipilimumab) 277305.5-5.50.572
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 275906.8-6.80.304
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21174.804.81
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)13117.707.71
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160001
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 3827011.1-11.10.067
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 221307.7-7.70.371
1529033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1614014.3-14.30.209
1629301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 11130001
1729301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 610001
1829301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 5120001
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of DCSTAMP. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene.
> Lymphocyte
 
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of DCSTAMP. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by DCSTAMP.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of DCSTAMP. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of DCSTAMP expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between DCSTAMP and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolDCSTAMP
Namedendrocyte expressed seven transmembrane protein
Aliases DC-STAMP; FIND; Dendritic cells (DC)-specific transmembrane protein; IL-Four INDuced; TM7SF4; transmembrane ......
Chromosomal Location8q22.3
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting DCSTAMP collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.